1. Volume 70, Issue 5, Pages 886-897 (June 2011)
Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders 
Dan Levy, Michael Ronemus, Boris Yamrom, Yoon-ha Lee, Anthony Leotta, Jude Kendall, Steven Marks, B. Lakshmi, Deepa Pai, Kenny Ye, Andreas Buja, Abba Krieger, Seungtai Yoon, Jennifer Troge, Linda Rodgers, Ivan Iossifov, Michael Wigler 
Neuron 
Volume 70, Issue 5, Pages (June 2011)
DOI: /j.neuron
Copyright © 2011 Elsevier Inc. Terms and Conditions

2. Figure 1 Data Processing Pipeline
The main data processing pipeline for identifying de novo and transmitted rare copy-number variants in the SSC is shown in gray at left, and the support pipeline, which includes quality control, is shown in white at right. Data sets are represented by boxes and computational processes by ovals. Raw ratio data were normalized and segmented prior to trio analysis. Supporting processes were used to determine hybridization quality, to exclude gender and pedigree mismatches, to establish probe filters, and to build models for various copy-number states.
Neuron  , DOI: ( /j.neuron )
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3. Figure 2 Noise Parameters and State Calls
Regions of common copy-number polymorphism in 3653 hybridizations were examined to validate the performance of signal and noise parameters. A commonly deleted region of 150 kb (representing a total of 99 probes) is displayed, along with the adjacent 20 probes from each flank.
(A) Median log ratio on the interval as a function of the signal parameter ξh. Magenta, red, and green curves correspond to the mean as predicted by the noise model for the three copy-number states 0, 1, and 2, respectively. The highlighted region to the right of the dashed line shows the values obtained in the 100 worst hybridizations.
(B and C) Probe log ratio values on the region for a subset of hybridizations. Experiments are sorted by the median probe ratio value of the polymorphic region. (B) shows 100 hybs selected at random from the left side of (A). (C) shows the 100 worst hybs from the highlighted (rightmost) region of (A).
(D)−(F) are as in (A)−(C) for the noise parameter σh.
Neuron  , DOI: ( /j.neuron )
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4. Figure 3 Ratio Data for De Novo Events
(A and B) Two representative de novo events, one duplication (A) and one deletion (B). In each panel, the mother's probe log ratio values appear in red, the father's in blue, and the proband's in green. Exons are shaded in green and purple, with colors alternating by gene (with gene names indicated in blue). Dashed horizontal lines show the mean ratios for the copy-number states 0, 1, 2, 3, and 4, as predicted by the noise parameters of the proband's hybridization. The boundaries of the deletion are indicated by the dashed vertical lines. The x axis gives the probe coordinates as an offset to the number in the lower right of the respective panel.
Neuron  , DOI: ( /j.neuron )
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5. Figure 4 Histogram of De Novo Gene Hits
Eighty-five children in the study had detectable de novo lesions: 33 had duplications, 49 had deletions, and three had both a deletion and a duplication. We determined the number of gene hits per child and aggregated by affected status and gender. The boundaries of the histogram bins are log scaled.
(A) Distribution of de novo deletions. Gender and affected status are shown in the box at upper right.
(B) Distribution of de novo duplications. Gender and affected status are as in (A).
Neuron  , DOI: ( /j.neuron )
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6. Figure 5 Distribution of De Novo Events in ASD Study Populations
A total of 75 de novo copy-number variants in autistic children were found in this study (designated by “L” in the legend). These observations were combined with the set of de novo CNVs identified in an earlier study (indicated by “P”) of similar scale (Pinto et al., 2010). Ten of the CNVs from the earlier study appeared to be common variants against the background of the SSC, and consequently were omitted (Table S6). Chromosomes are pictured with alternating dark and light regions for each cytoband and aligned by centromeres. Duplications are pictured above and deletions below the respective chromosomal locus. Events in males and females from the SSC study (“L”) appear in blue and red, respectively. Events in males and females from the Pinto et al. (2010) study (“P”) appear in light blue and light red, respectively. Green bars spanning chromosomes indicate the positions of the 12 loci with recurrent de novo events.
Neuron  , DOI: ( /j.neuron )
Copyright © 2011 Elsevier Inc. Terms and Conditions